Journal of Bacteriology, September 1998, p. 4903-4911, Vol. 180, No. 18
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Department of Microbiology and the Plant Molecular Biology/Biotechnology Program, The Ohio State University, Columbus, Ohio 43210-1292
Received 30 December 1997/Accepted 21 July 1998
A number of
cbbFI::lacZ translational
fusion plasmids containing various lengths of sequence 5' to the form I
(cbbI) Calvin-Benson-Bassham cycle operon
(cbbFIcbbPIcbbAIcbbLIcbbSI)
of Rhodobacter sphaeroides were constructed. Expression of
-galactosidase was monitored under a variety of growth conditions.
It was found that 103 bp of sequence upstream of the
cbbFI transcription start was sufficient to
confer low levels of regulated cbbI promoter
expression; this activity was dependent on the presence of an intact
cbbR gene. Additionally, R. sphaeroides
CbbR was shown to bind to the region between 9 and 100 bp 5' to the
cbbFI transcription start. Inclusion of an
additional upstream sequence, from 280 to 636 bp 5' to
cbbFI, resulted in a significant increase in
regulated cbbI promoter expression under all
growth conditions tested. A 50-bp region responsible for the majority
of this increase occurs between 280 and 330 bp 5' to
cbbFI. The additional 306 bp of upstream
sequence from 330 to 636 bp also appears to play a positive regulatory role. A 4-bp deletion 281 to 284 bp 5' to cbbFI
significantly reduced cbbI expression while the
proper regulatory pattern was retained. These studies provide evidence
for the presence of two functionally distinct regions of the
cbbI promoter, with the distal domain providing
significant regulated promoter activity that adheres to the normal
pattern of expression.
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